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NCT00433953 · ClinicalTrials.gov registry record · Phase 1

Genetic Drug Study of Mycophenolic Acid (CellCept) in Pediatric Kidney Transplant Patients

A Phase 1 study, sponsored by Children's Hospital Medical Center, Cincinnati.

Terminated
Registry status
Phase 1
Development phase
44
Enrollment target

NCT00433953: Clinical Trial Phase 1 study, sponsored by Children's Hospital Medical Center, Cincinnati.

NCT00433953 is a Phase 1 study that was terminated before completion, run by Children's Hospital Medical Center, Cincinnati. The registered enrollment target is 44 participants, below the 60-participant average among 29,502 other Phase 1 trials with a reported enrollment target (27% lower). According to ClinicalTrials.gov, the official US trial registry.

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The verdict

NCT00433953, a Phase 1 study, was terminated before completion, sponsored by Children's Hospital Medical Center, Cincinnati.

TERMINATED
Registry status
Phase 1
Development phase
44 participants
Enrollment target

Study Summary

The purpose of this study is to determine how genes influence the response to mycophenolate mofetil (CellCept) in children who have had a kidney transplant. The study will look at how differences in some genes effect blood levels of mycophenolate mofetil over time in children, how often side effects occur and the way that children respond to mycophenolate mofetil. The results may lead to better dosing based on individual needs.

Interventions

  • BEHAVIORAL Dietary Monitoring
  • PROCEDURE Blood Sampling
  • BEHAVIORAL Drug Diary
  • DRUG Mycophenolate Mofetil (CellCept)

Trial Details

FieldValue
Enrollment Target 44 participants
Start Date 2007-02
Est. Completion 2010-02
Phase Phase 1

Why NCT00433953 stopped before completion

NCT00433953 is an interventional study that assigns participants to a tested intervention. The registry caps enrollment at 44 participants, a relatively small participant target, below the 60-participant average among 29,502 other Phase 1 trials with a reported enrollment target (27% lower).

The record links to 0 conditions, and to 4 interventions - of which Dietary Monitoring is the first listed.

NCT00433953 does not publish any study locations in the registry export this page uses.

Frequently Asked Questions

What is clinical trial NCT00433953 about?

NCT00433953 is a clinical study titled "Genetic Drug Study of Mycophenolic Acid (CellCept) in Pediatric Kidney Transplant Patients". The purpose of this study is to determine how genes influence the response to mycophenolate mofetil (CellCept) in children who have had a kidney transplant. The study will look at how differences in some genes effect blood levels of mycophenolate mofetil over time in children, how often side effects...

What is the current status of trial NCT00433953?

This trial is currently terminated. It is a Phase 1 study. The enrollment target is 44 participants. The study started on 2007-02. Estimated completion is 2010-02.

What interventions are being tested in trial NCT00433953?

The interventions under investigation include: Dietary Monitoring (BEHAVIORAL), Blood Sampling (PROCEDURE), Drug Diary (BEHAVIORAL), Mycophenolate Mofetil (CellCept) (DRUG).

Who is sponsoring clinical trial NCT00433953?

This trial is sponsored by Children's Hospital Medical Center, Cincinnati, which has 571 total clinical trials registered on ClinicalTrials.gov.

How this trial's enrollment target compares

Where NCT00433953's enrollment target sits among peer trials

44 1086th of 2000 higher than 901 of 2,000 other Phase 1 trials

participants (enrollment target), bucketed by value

Each bar is a band; taller bars hold more other Phase 1 trials. The dashed line + filled bar mark this entry. Hover or tap any bar for its full count and share, and where it sits relative to this entry.

Source ClinicalTrials.gov registry export · 2026-08-08

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Source: ClinicalTrials.gov NCT00433953, the US trial registry maintained by the National Library of Medicine. NCT00433953 (small enrollment · none site footprint · terminated) retrieved and formatted by PlainTrial, see methodology.